Marchio A, Meddeb M, Pineau P, Danglot G, Tiollais P, Bernheim A, Dejean A
Unité de Recombinaison et Expression Génétique, INSERM U163, Institut Pasteur, Paris, France.
Genes Chromosomes Cancer. 1997 Jan;18(1):59-65.
Comparative genomic hybridization (CGH) was used to evaluate and map genomic aberrations in 50 hepatocellular carcinomas (HCCs) from patients chronically infected with hepatitis B virus (HBV). CGH clearly detected nonrandom genomic imbalances. Losses were most prevalent on chromosome regions 4q (70%), 8p (65%), 16q (54%), 17p (51%), 13q and 6q (37% each), and lp (30%). The most frequent gains occurred on 8q (60%), 1q (58%), and 6p and 17q (33% each). In a few cases, sequence amplifications were detected that were mapped to bands 11q12, 12p11, 14q12, and 19q13.1. This study represents the first analysis of primary liver cancers by CGH, and it confirms the presence of previously known chromosomal aberrations in HCC and highlights new quantitative abnormalities and sequence amplifications. These findings should lead to the characterization of new loci involved in liver cancer pathogenesis.
采用比较基因组杂交(CGH)技术对50例慢性乙型肝炎病毒(HBV)感染患者的肝细胞癌(HCC)进行基因组畸变评估和定位。CGH能清晰检测到非随机的基因组失衡。缺失最常见于4q(70%)、8p(65%)、16q(54%)、17p(51%)、13q和6q(各37%)以及1p(30%)染色体区域。最常见的扩增发生在8q(60%)、1q(58%)以及6p和17q(各33%)。在少数病例中,检测到序列扩增,定位于11q12、12p11、14q12和19q13.1带。本研究是首次采用CGH对原发性肝癌进行分析,证实了HCC中存在先前已知的染色体畸变,并突出了新的数量异常和序列扩增。这些发现应有助于确定参与肝癌发病机制的新基因座。